CasNo: 294-90-6
Molecular Formula: C8H20N4
Appearance: off- white to slightly yellow crystalline powder
Chemical Properties |
ALMOST WHITE TO SLIGHTLY YELLOW CRYSTALLINE POWDER |
Uses |
Macrocyclic aza analogue of the crown ether 12-crown-4. Cyclen compounds are capable of selectively binding cations and are used as a ligand with chemicals used in MRI contrast (as well ass other imaging) agents. The use of cyclen (1,4,7,10-tetraazacyclododecane) as a blocking ligand enables assembly of the mixed-valence square complex [(cyclen) 4 Ru 4 (pz) 4 ] 9+ (pz = pyrazine). |
General Description |
Cyclen is a microcyclic tetramine that can be used as a ligand that forms a co-ordination linkage with the surface metal cations. It can be used as a synthetic precursor. It can be prepared by S-alkylation of dithiooxamide with an excess amount of bromoethane. |
Flammability and Explosibility |
Notclassified |
InChI:InChI=1/C8H20N4/c1-2-10-5-6-12-8-7-11-4-3-9-1/h9-12H,1-8H2/p+4
Specifically, precisely regulated NF membranes were prepared through a conventional IP process with Cyclen as the structural regulator, as well as PEI and TMC as the reactive monomers.
A zine(II) complex of acridine-pendant cyclen, 4.2ClO4 (cyclen=1.4.7,10-tetraazacyclododecane, 1), has been designed and synthesized as a new "multipoint" nucleobase receptor molecule in aqueous solution at physiological pH and compared with a Znll pendantless cyclen complex 2 recently discovered (ref 9) as a highly slective host for dT (deoxythymidine) and U (uridine).
In this work, hydrogen peroxide disproportionation using complexes formed between manganese and cyclen or pyclen were investigated due to the spectroscopic similarities with the native MnCAT enzyme.
C14H24N4
cyclohexane-1,2-dione
1,4,7,10-tetraazacyclododecan
Conditions | Yield |
---|---|
With hydrogenchloride; In water; at 60 ℃; for 6h;
|
1,4,7,10-tetraazacyclododecane tetrahydrochloride
1,4,7,10-tetraazacyclododecan
Conditions | Yield |
---|---|
With hydrogenchloride;
|
95% |
With potassium hydroxide; In water; at 0 - 10 ℃;
|
91.3% |
With potassium hydroxide;
|
|
With sodium hydroxide; In toluene; at 40 ℃; for 1h; Reflux;
|
13.77 g |
With sodium hydroxide; In water; toluene;
|
12 g |
1,4,7,10-tetraazacyclododecane tetrahydrochloride
7-<2-(1,3-Dioxolan-2-yl)ethyl>-1,4,7,10-tetraazacyclododecane-1-carbaldehyde
cyclen tetratosylate
cis-octahydro-2a,4a,6a,8a-tetraazacyclopenta[fg]acenaphthylene-3,4-dione
1-benzyl-1,4,7,10-tetraazacyclododecane
1,4,7,10-tetrazatricyclo[5.5.1.0]tridecane
1,4,7,10-tetraazacyclododecane-1,4,7-triacetic acid
1,4,7-tribenzyl 1,4,7,10-tetraazacyclododecane 1,4,7-tricarboxylate
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